Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:38388143-38388429 | Common:1; Rare:62 | ||||
chr19:38388473-38388744 | Rare:63 | ||||
chr19:38402929-38403251 | Common:6; Rare:109 | ||||
chr19:38433540-38433729 | Common:2; Rare:36; Clinvar (benign):2 | ||||
chr19:38595985-38596363 | Rare:105 | ||||
chr19:38596479-38596838 | Common:2; Rare:79 | ||||
chr19:38618912-38619323 | Common:3; Rare:115 | ||||
chr19:38647367-38647845 | Common:3; Rare:158 | ||||
chr19:38648286-38648795 | Common:3; Rare:97 | ||||
chr19:38736630-38737124 | Common:7; Rare:107 | ||||
chr19:38831094-38831313 | Common:2; Rare:78 | ||||
chr19:38831755-38831959 | Common:4; Rare:75; Clinvar (benign):1 | ||||
chr19:38842131-38842526 | Rare:81 | ||||
chr19:38842602-38842732 | Rare:25 | ||||
chr19:38849441-38849464 | Rare:4 |